440351-19-9

Upstream product

• 440351-18-8 (3aR,3bS,8S,8aR,9aR)-8-(3-Benzyloxy-butyl)-2,2,5,5-tetramethyl-hexahydro-1,3,4,6,9-pentaoxa-cyclopenta[a]azulene 
• 440351-17-7 4-((3aR,3bS,8S,8aR,9aR)-2,2,5,5-Tetramethyl-hexahydro-1,3,4,6,9-pentaoxa-cyclopenta[a]azulen-8-yl)-butan-2-ol 
• 440351-16-6 3-((3aR,3bS,8S,8aR,9aR)-2,2,5,5-Tetramethyl-hexahydro-1,3,4,6,9-pentaoxa-cyclopenta[a]azulen-8-yl)-propan-1-ol 
• 440351-14-4 (3aR,3bS,8S,8aR,9aR)-8-Allyl-2,2,5,5-tetramethyl-hexahydro-1,3,4,6,9-pentaoxa-cyclopenta[a]azulene 
• 440351-13-3 5-C-allyl-5-deoxy-1,2-O-isopropylidene-β-L-idofuranose 
• 440351-12-2 5-C-allyl-5-deoxy-1,2-O-isopropylidene-β-L-idofuranurono-6,3-lactone 
• 57569-46-7 5-chloro-5-deoxy-1,2-O-isopropylidene-β-L-idofuranuronic acid-3,6-lactone 

Downstream Products

• 440351-20-2 (3aR,5R,6S,6aR)-5-[(S)-4-Benzyloxy-1-(tert-butyl-dimethyl-silanyloxymethyl)-pentyl]-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-ol 
• 440351-23-5 (3aR,5R,6R,6aR)-5-[(S)-4-Benzyloxy-1-(tert-butyl-dimethyl-silanyloxymethyl)-pentyl]-2,2,6-trimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-ol 
• 440351-26-8 [(S)-5-Benzyloxy-2-((3aR,5R,6aR)-2,2-dimethyl-6-methylene-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-hexyloxy]-tert-butyl-dimethyl-silane 
• 440351-33-7 [(S)-5-Benzyloxy-2-((3aR,5S,6aR)-2,2-dimethyl-6-methylene-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-hexyloxy]-tert-butyl-dimethyl-silane 
• 440351-30-4 (3aR,5S,6S,6aR)-5-[(S)-4-Benzyloxy-1-(tert-butyl-dimethyl-silanyloxymethyl)-pentyl]-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-ol 
• 440351-22-4 (3aR,5R,6aS)-5-[(S)-4-Benzyloxy-1-(tert-butyl-dimethyl-silanyloxymethyl)-pentyl]-2,2-dimethyl-dihydro-furo[2,3-d][1,3]dioxol-6-one 
• 440351-35-9 [(S)-5-Benzyloxy-2-((3aR,5S,6R,6aR)-2,2,6-trimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-hexyloxy]-tert-butyl-dimethyl-silane 
• 440351-28-0 [5-benzyloxy-2-(2,2-dimethyl-3a,6a-dihydro-furo[2,3-d][1,3]dioxol-5-yl)-hexyloxy]-tert-butyl-dimethyl-silane 

Relevant academic research and scientific papers

A stereoselective synthesis of the C13-C19 fragment of sanglifehrin A

A stereo-controlled radical C-C bond formation involving a 5-chloro-5-deoxy-L-idofurano-6,3-lactone derivative and allyltri-n-butyltin/AIBN is described. Further elaboration led to the synthesis of the C13-C19 segment of sanglifehrin A.